MadSci Network: Chemistry |
I think I understand the overall reaction but I am puzzled by the acid. My initial thoughts are that the acid will protonate the carbonyl oxygen atom of the carboxylic acid group to produce a diol carbocation. This can then be attacked by the unbonded electron pair of the nitrogen in the amine group of the benzyl diamine component. I just dont understand why nucleophilic attack of the carbonyl carbon atom cannot take place without protonation leading to the carbocation formation. Is the amine group not nucleophilic enough as it is? Or am I not understanding the function of the acid?
Re: What is the function of the acid in the polymerisation of kevlar?
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